McNiven Mark A, Baldassarre Massimiliano, Buccione Roberto
Department of Biochemistry and Molecular Biology, Center for Basic Research in Digestive Diseases, Mayo Clinic, Rochester, MN, USA.
Front Biosci. 2004 May 1;9:1944-53. doi: 10.2741/1348.
Cells make contact with the extracellular matrix (ECM) through extensions of the plasma membrane; these range from irregular dynamic structures, e.g. lamellipodia, ruffles and pseudopodia, to more localized and highly defined protrusions, e.g. podosomes and invadopodia. Both might be instruments through which cells sample the immediate extracellular environment and maintain polarized activities such as chemotaxis and focal degradation of the matrix. Podosomes are expressed in cells of the monocytic lineage, and most studies point to a role for podosomes in adhesion/motility. Invadopodia are prominent in certain aggressive cancer cells (or transformed cells) and appear to be directly responsible for focal ECM degradation. Recent studies have revived interest in these structures in terms of the actin regulation machinery. Within this framework, the atypical GTP-binding protein dynamin, a central modulator of protrusive events, has been associated to podosome and invadopodia structure and function. Here, we specifically discuss the role played by dynamin in controlling the activities and function of these structures.
细胞通过质膜延伸与细胞外基质(ECM)接触;这些延伸结构范围从不规则的动态结构,如片状伪足、褶皱和伪足,到更局部化且高度明确的突起,如足体和侵袭性伪足。两者都可能是细胞用于探测紧邻的细胞外环境并维持诸如趋化作用和基质局部降解等极化活动的工具。足体在单核细胞谱系的细胞中表达,大多数研究表明足体在黏附/运动中发挥作用。侵袭性伪足在某些侵袭性癌细胞(或转化细胞)中很突出,似乎直接负责局部ECM降解。近期研究就肌动蛋白调节机制而言重新引发了对这些结构的兴趣。在此框架内,非典型GTP结合蛋白发动蛋白作为突出事件的核心调节因子,已与足体和侵袭性伪足的结构及功能相关联。在这里,我们具体讨论发动蛋白在控制这些结构的活动和功能中所起的作用。